Aged female mice lacking the Terf2 gene, encoding the telomeric protective factor TRF2, in their skeletal myofibers exhibit a younger muscle phenotype with lack of ongoing or past regeneration and myofiber atrophy, preserved muscle strength, and moderate prolonged lifespan. Since this is accompanied by a slight pro-oxidant effect without telomere deprotection, we propose that the age-related TRF2 downregulation triggers a mito-hormetic response with beneficial effect in the skeletal muscle.
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Burbano et al. (2024) studied this question.
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